The development of cellular systems for the screening of molecules able to induce the production of fetal or adult hemoglobin in crythroid cells isolated from beta-thalassemia patients is very important for the identification of molecules of interest for pharmacological therapy of thalassemia. This article reports the development of a cellular system for the identification of inducers of fetal hemoglobin preferentially acting on the human gamma-globin gene promoter. To achieve this aim, green and red fluorescence protein genes were cloned under the control of gamma-globin and beta-globin promoters, respectively. The developed K562 clones were tested for the increase of fluorescence after treatment with sodium butyrate and hydroxyurea, two well-known inducers of fetal hemoglobin.
Cellular biosensors for the identification of fetal hemoglobin inducers
BREVEGLIERI, Giulia;SALVATORI, Francesca;FINOTTI, Alessia;DESTRO, Federica;FALZONI, Simonetta;BIANCHI, Nicoletta;BORGATTI, Monica;ZUCCATO, Cristina;FERIOTTO, Giordana;GAMBARI, Roberto
2007
Abstract
The development of cellular systems for the screening of molecules able to induce the production of fetal or adult hemoglobin in crythroid cells isolated from beta-thalassemia patients is very important for the identification of molecules of interest for pharmacological therapy of thalassemia. This article reports the development of a cellular system for the identification of inducers of fetal hemoglobin preferentially acting on the human gamma-globin gene promoter. To achieve this aim, green and red fluorescence protein genes were cloned under the control of gamma-globin and beta-globin promoters, respectively. The developed K562 clones were tested for the increase of fluorescence after treatment with sodium butyrate and hydroxyurea, two well-known inducers of fetal hemoglobin.I documenti in SFERA sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.